NDC 80725-005

Valium

Diazepam

Valium is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Waylis Therapuetics Llc. The primary component is Diazepam.

• Product ID: 80725-005_dc250376-39ef-2207-e053-2a95a90a4901
• NDC: 80725-005
• Product Type: Human Prescription Drug
• Proprietary Name: Valium
• Generic Name: Diazepam
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2022-04-04
• Marketing Category: NDA /
• Application Number: NDA013263
• Labeler Name: Waylis Therapuetics LLC
• Substance Name: DIAZEPAM
• Active Ingredient Strength: 5 mg/1
• Pharm Classes: Benzodiazepine [EPC], Benzodiazepines [CS]
• DEA Schedule: CIV
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 80725-005-01

100 TABLET in 1 BOTTLE (80725-005-01)

• Marketing Start Date: 2022-04-04
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "Valium" or generic name "Diazepam"

NDC	Brand Name	Generic Name
0140-0004	Valium	diazepam
0140-0005	Valium	diazepam
0140-0006	Valium	diazepam
55289-117	Valium	Valium
65084-313	Valium	Valium
65084-312	Valium	Valium
80425-0120	Valium	Valium
0187-0658	Diastat	diazepam
0187-0659	Diastat	diazepam
0054-3188	Diazepam	Diazepam
0093-6137	Diazepam	Diazepam
0093-6138	Diazepam	Diazepam
0093-6139	Diazepam	Diazepam
0121-0905	Diazepam	Diazepam
0172-3925	Diazepam	Diazepam
0172-3926	Diazepam	Diazepam
0172-3927	Diazepam	Diazepam